Symptomatology during previous SARS-CoV-2 infection and serostatus before vaccination influence the immunogenicity of BNT162b2 COVID-19 mRNA vaccine.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 27 04 2022
accepted: 20 09 2022
entrez: 31 10 2022
pubmed: 1 11 2022
medline: 2 11 2022
Statut: epublish

Résumé

Public health vaccination recommendations for COVID-19 primary series and boosters in previously infected individuals differ worldwide. As infection with SARS-CoV-2 is often asymptomatic, it remains to be determined if vaccine immunogenicity is comparable in all previously infected subjects. This study presents detailed immunological evidence to clarify the requirements for one- or two-dose primary vaccination series for naturally primed individuals. The main objective was to evaluate the immune response to COVID-19 mRNA vaccination to establish the most appropriate vaccination regimen to induce robust immune responses in individuals with prior SARS-CoV-2 infection. The main outcome measure was a functional immunity score (zero to three) before and after vaccination, based on anti-RBD IgG levels, serum capacity to neutralize live virus and IFN-γ secretion capacity in response to SARS-CoV-2 peptide pools. One point was attributed for each of these three functional assays with response above the positivity threshold. The immunity score was compared based on subjects' symptoms at diagnosis and/or serostatus prior to vaccination. None of the naïve participants (n=14) showed a maximal immunity score of three following one dose of vaccine compared to 84% of the previously infected participants (n=55). All recovered individuals who did not have an immunity score of three were seronegative prior to vaccination, and 67% had not reported symptoms resulting from their initial infection. Following one dose of vaccine, their immune responses were comparable to naïve individuals, with significantly weaker responses than individuals who were symptomatic during infection. These results indicate that the absence of symptoms during initial infection and negative serostatus prior to vaccination predict the strength of immune responses to COVID-19 mRNA vaccine. Altogether, these findings highlight the importance of administering the complete two-dose primary regimen and following boosters of mRNA vaccines to individuals who experienced asymptomatic SARS-CoV-2 infection.

Identifiants

pubmed: 36311736
doi: 10.3389/fimmu.2022.930252
pmc: PMC9614167
doi:

Substances chimiques

COVID-19 Vaccines 0
BNT162 Vaccine 0
Viral Vaccines 0
RNA, Messenger 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

930252

Subventions

Organisme : NIAID NIH HHS
ID : 75N93019C00065
Pays : United States

Informations de copyright

Copyright © 2022 Nantel, Bourdin, Adams, Carbonneau, Rabezanahary, Hamelin, McCormack, Savard, Longtin, Cheng, De Serres, Corbeil, Gilca, Baz, Boivin, Quach and Decaluwe.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Sabryna Nantel (S)

Cytokines and Adaptive Immunity Lab, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Microbiology, Infectiology and Immunology Department, Faculty of Medicine, University of Montréal, Montréal, QC, Canada.

Benoîte Bourdin (B)

Cytokines and Adaptive Immunity Lab, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.

Kelsey Adams (K)

Clinical Department of Laboratory Medicine, Infection Prevention and Control, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.

Julie Carbonneau (J)

Infectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.

Henintsoa Rabezanahary (H)

Infectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Microbiology, Infectiology and Immunology Department, Université Laval, Québec City, QC, Canada.

Marie-Ève Hamelin (MÈ)

Infectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.

Deirdre McCormack (D)

Clinical Department of Laboratory Medicine, Infection Prevention and Control, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.

Patrice Savard (P)

Microbiology, Infectiology and Immunology Department, Faculty of Medicine, University of Montréal, Montréal, QC, Canada.
Immunopathology Department, Montreal University Hospital and Research Center, Montréal, QC, Canada.

Yves Longtin (Y)

Infectious Diseases Service, Department of Medicine, Jewish General Hospital, Montréal, QC, Canada.

Matthew P Cheng (MP)

Biological and Occupational Risk, Divisions of Infectious Diseases and Medical Microbiology, Departments of Medicine and Laboratory Medicine, McGill University Health Center, Montréal, QC, Canada.

Gaston De Serres (G)

Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Biological and Occupational Risk, Institut National de Santé Publique du Québec, Québec City, QC, Canada.
Preventive and Social Medicine Department, Université Laval, Québec City, QC, Canada.

Jacques Corbeil (J)

Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Molecular Medicine Department, Université Laval, Québec City, QC, Canada.

Vladimir Gilca (V)

Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Biological and Occupational Risk, Institut National de Santé Publique du Québec, Québec City, QC, Canada.
Preventive and Social Medicine Department, Université Laval, Québec City, QC, Canada.

Mariana Baz (M)

Infectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.
Microbiology, Infectiology and Immunology Department, Université Laval, Québec City, QC, Canada.

Guy Boivin (G)

Infectious Disease Research Center, Université Laval, Québec City, QC, Canada.
Centre Hospitalier Universitaire de Québec - Université Laval Research Center, Québec City, QC, Canada.

Caroline Quach (C)

Microbiology, Infectiology and Immunology Department, Faculty of Medicine, University of Montréal, Montréal, QC, Canada.
Clinical Department of Laboratory Medicine, Infection Prevention and Control, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.

Hélène Decaluwe (H)

Cytokines and Adaptive Immunity Lab, Sainte-Justine University Hospital and Research Center, Montréal, QC, Canada.
Microbiology, Infectiology and Immunology Department, Faculty of Medicine, University of Montréal, Montréal, QC, Canada.
Pediatric Immunology and Rheumatology Division, Department of Pediatrics, University of Montréal, Montréal, QC, Canada.

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